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During late pregnancy in rats, hormonal changes increased certain GABAA receptors in specific brain cells.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

Gene expression affects fur development in rex rabbits.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Foxn1 is essential for hair pigmentation by directing pigment transfer to hair cells.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

Dormant melanoma cells in mice interact minimally with memory T cells due to a suppressive tumor environment.

Desmocollin 1 is essential for strong skin and proper skin function.

Ets2 gene is crucial for placental development in mice.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

The EDAR V370A allele in East Asians likely evolved due to reliance on aquatic resources providing essential nutrients.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

The EDAR V370A allele in East Asians likely evolved due to reliance on aquatic resources providing essential nutrients.

Inhibiting retinoic acid activates WNT signaling, potentially aiding hair disorder and skin cancer treatments.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Enhancing Tregs can protect against alopecia areata.

Sex steroids affect the MafB gene differently in male and female hamsters.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

HoxC genes are crucial for normal hair and nail development.

Mice with enhanced regeneration abilities may help develop new regenerative medicine therapies.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.